| Tag | Content |
|---|
EnhancerAtlas ID | HS157-08972 |
Organism | Homo sapiens |
Tissue/cell | PANC-1 |
Coordinate | chr2:234739000-234740050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr2:234739716-234739726 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr2:234739716-234739726 | GACACGTGCC | - | 6.02 | | RREB1 | MA0073.1 | chr2:234739051-234739071 | GGGAGGTGGCTGATTTGGGG | - | 6.48 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTTCTCTCCC TAGTCTCTGC TTACAGACTT GGGGGGTGGG GTCAGGAAGT GGGGAGGTGG 60
CTGATTTGGG GAGGTTCTGC CCCCGCCTAG TAAGCCTTGG GACGCAGCTG GCCTAACATG 120
AAAGAAATGC AATGGTCATT TTCAGCAGGT GCCTTGGACT CCAGCTCTGG GGTCACAGGA 180
CAAGTACTGT CACTATGAGG GCAGCAGTTT CCAGGTGGGG TGGAGCGGGT GGCCCAGATG 240
GCCTGGGTGG CCCAGGTGGG ATGGCCCAGG TGGCCCAGGT GGGATGGCCC TGGTGGCCCA 300
GGTGGGATGG CCCAGGTGGC CCTTACAGGC AGTGAGGGGG ATTGAGATGC ACACTCCCTA 360
GACCTGGGCT TTGCACTCAC CACCCCAGCT TCTGGACTTT GCCACATCCC TCTGCCACAC 420
CATCCCTGGC CACCCTGGGC ACAAGGTGTC ACTGCCCAGA GGCTCCTTTT CCTTGCCAGT 480
CCTCACCACC CTCTGTCTTC AGCCCACACT GTTCTTCCAT GTTTTATCGA CAACTGTCCA 540
GTGGGGTGGG GGGGCTTCAG GGAAGGAACC AGGGTGCACC CAGCAATGGT GACCGAGAGT 600
GAGGAAAGGG CTACCGAGAC AGAAGCATTT TGTCTTCCTG CCCTGCCGTC TCCAGAAGCT 660
GTGGCCAGCA GGCTTGGTCA CAGGCAGATG CTGGTGGACT GGGCCTGGGA GGTGAGGACA 720
CGTGCCCAGT CTTGCCTGCT CAAGCCCGGC TCCCGCCTCT GATCCCATGG AGGGCTGGGT 780
CCCAGGCAGG GCTGCTGAGG GCACGAAGGT GCTGGCTGAG GGGGCGGGTG GGGCTGCATC 840
TGCCCCCAAG GGGCTTTCTA TAAATGTACC TGCAGCCATG TTCAAGCTGG CAGGGGCCCA 900
GGTCCCAGGT GGCCTCCCAG GAGCCACCAG CCCTGCCTTT CTTTGGCTTG GTGAGGCTTT 960
TCTGGGGCTG CCCTCTGGCT TCCTGCCAGC CTCACCCCTC TGGGGAACCA CGTGGCCTGG 1020
CTGATGGCTC TGCTGCCGTC CTGTGTCCCT 1050
|
